Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37197
Title: Peripheral blood mononuclear cell microRNAs in coronary artery disease
Authors: Sanlialp, M.
Dodurga, Yavuz
Uludag, B.
Alihanoglu, Y.I.
Enli, Yaşar
Seçme, Mücahit
Bostanci, H.E.
Keywords: CAD
lipoprotein A
miRNA
angiotensin receptor antagonist
beta adrenergic receptor blocking agent
biological marker
dipeptidyl carboxypeptidase inhibitor
hydroxymethylglutaryl coenzyme A reductase inhibitor
microRNA
microRNA 145
microRNA 155
microRNA 21
microRNA 221
nitrate
adult
aged
Article
biochemical analysis
controlled study
coronary angiography
coronary artery bypass surgery
coronary artery disease
coronary artery obstruction
down regulation
enzyme linked immunosorbent assay
female
gene expression
human
hypertension
major clinical study
male
people by smoking status
percutaneous coronary intervention
peripheral blood mononuclear cell
priority journal
real time polymerase chain reaction
RNA isolation
Publisher: Wiley-Liss Inc.
Abstract: The accuracy of risk prediction for coronary artery disease can be improved with the use of novel molecular or genetic biomarkers. In this study, we investigated the difference of five selected microRNAs (miR or miRNA) in patients with coronary artery disease (CAD) and controls, assessed by coronary angiography. The study population consisted of 85 subjects, aged between 18 and 75 years and underwent invasive coronary angiography. Subjects with more than 30% stenosis in at least one coronary artery, patients with a history of prior percutaneous coronary intervention or coronary by-pass surgery were allocated to the patient group; whereas the subjects without at least 30% stenosis consisted the control group. Groups were similar in age, presence of hypertension, and smoking status. However, the proportion of males and subjects taking angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta blockers, nitrates, and statins were higher in the patient group. miR-221 and miR-155 were downregulated (P =.02 and.001, respectively), while miR-21 levels were significantly increased (P =.003) in the patient group compared to controls. Changes in miR-145 and miR-126 did not reach statistical significance (P >.05). miRNA- 21, miR-155, and miR-221 were differentially expressed between the patients and controls. miRNAs are promising biomarkers for CAD diagnosis, however, this requires further research with larger groups. © 2019 Wiley Periodicals, Inc.
URI: https://hdl.handle.net/11499/37197
https://doi.org/10.1002/jcb.29557
ISSN: 0730-2312
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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